RU2313541C2 - Способ приготовления стабильных водных дисперсий поликарбодиимидов, которые не содержат органических растворителей и могут быть использованы в качестве поперечно-сшивающих агентов - Google Patents

Способ приготовления стабильных водных дисперсий поликарбодиимидов, которые не содержат органических растворителей и могут быть использованы в качестве поперечно-сшивающих агентов Download PDF

Info

Publication number: RU2313541C2
Authority: RU; Russia
Prior art keywords: polycarbodiimide; diisocyanate; mixture; formation; polyisocyanate
Prior art date: 2003-07-03

Application number

RU2005141416/04A

Other languages

English (en)

Russian (ru)

Other versions

RU2005141416A (ru

Inventor

Лаурентиус Корнелиус Йосеф ХЕССЕЛМАНС (NL)

Лаурентиус Корнелиус Йосеф ХЕССЕЛМАНС

Андрис Йоханнес ДЕРКСЕН (NL)

Андрис Йоханнес ДЕРКСЕН

Якоб Христиан МЮННЕКЕ (NL)

Якоб Христиан МЮННЕКЕ

Original Assignee

Стахл Интернэшнл Б.В.

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2003-07-03

Filing date

2004-07-02

Publication date

2007-12-27

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33563077&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=RU2313541(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2004-07-02 Application filed by Стахл Интернэшнл Б.В. filed Critical Стахл Интернэшнл Б.В.

2006-08-10 Publication of RU2005141416A publication Critical patent/RU2005141416A/ru

2007-12-27 Application granted granted Critical

2007-12-27 Publication of RU2313541C2 publication Critical patent/RU2313541C2/ru

Links

239000006185 dispersion Substances 0.000 title claims abstract description 31
238000000034 method Methods 0.000 title claims abstract description 16
239000003431 cross linking reagent Substances 0.000 title claims abstract description 10
239000003960 organic solvent Substances 0.000 title claims abstract description 5
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 27
239000000203 mixture Substances 0.000 claims abstract description 25
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
230000015572 biosynthetic process Effects 0.000 claims abstract description 20
150000001718 carbodiimides Chemical class 0.000 claims abstract description 16
150000001875 compounds Chemical class 0.000 claims abstract description 15
239000003054 catalyst Substances 0.000 claims abstract description 11
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims abstract description 11
239000005056 polyisocyanate Substances 0.000 claims abstract description 11
229920001228 polyisocyanate Polymers 0.000 claims abstract description 11
239000000872 buffer Substances 0.000 claims abstract description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 10
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims abstract description 9
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims abstract description 9
150000002009 diols Chemical class 0.000 claims abstract description 9
150000004985 diamines Chemical class 0.000 claims abstract description 8
125000005270 trialkylamine group Chemical group 0.000 claims abstract description 6
-1 dialkylaminoalkyl alcohol Chemical compound 0.000 claims abstract description 5
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims abstract description 5
239000005059 1,4-Cyclohexyldiisocyanate Substances 0.000 claims abstract description 3
ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 claims abstract description 3
238000001704 evaporation Methods 0.000 claims abstract description 3
239000000463 material Substances 0.000 claims abstract description 3
239000000758 substrate Substances 0.000 claims abstract description 3
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims abstract description 3
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims abstract description 3
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract 5
125000001931 aliphatic group Chemical group 0.000 claims abstract 4
125000003118 aryl group Chemical group 0.000 claims abstract 4
229920005862 polyol Polymers 0.000 claims description 14
150000003077 polyols Chemical class 0.000 claims description 14
239000002585 base Substances 0.000 claims description 10
229920000768 polyamine Polymers 0.000 claims description 8
238000000576 coating method Methods 0.000 claims description 7
239000011347 resin Substances 0.000 claims description 7
229920005989 resin Polymers 0.000 claims description 7
IUUONVQOMMQAEH-UHFFFAOYSA-N 1-methyl-2,3-dihydro-1$l^{5}-phosphole 1-oxide Chemical group CP1(=O)CCC=C1 IUUONVQOMMQAEH-UHFFFAOYSA-N 0.000 claims description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
239000011248 coating agent Substances 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
239000004721 Polyphenylene oxide Substances 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
125000000524 functional group Chemical group 0.000 claims description 3
229920000570 polyether Polymers 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
229920002292 Nylon 6 Polymers 0.000 claims description 2
150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
229920000515 polycarbonate Polymers 0.000 claims description 2
239000004417 polycarbonate Substances 0.000 claims description 2
229920005906 polyester polyol Polymers 0.000 claims description 2
150000003512 tertiary amines Chemical class 0.000 claims description 2
125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
239000000126 substance Substances 0.000 abstract 7
CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 abstract 1
230000008034 disappearance Effects 0.000 abstract 1
230000008020 evaporation Effects 0.000 abstract 1
230000003993 interaction Effects 0.000 abstract 1
229910000000 metal hydroxide Inorganic materials 0.000 abstract 1
150000004692 metal hydroxides Chemical class 0.000 abstract 1
125000005442 diisocyanate group Chemical group 0.000 description 4
239000000243 solution Substances 0.000 description 4
238000003756 stirring Methods 0.000 description 4
UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
238000002329 infrared spectrum Methods 0.000 description 3
239000012948 isocyanate Substances 0.000 description 3
150000002513 isocyanates Chemical class 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
239000007787 solid Substances 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
239000005058 Isophorone diisocyanate Substances 0.000 description 2
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 2
IIGAAOXXRKTFAM-UHFFFAOYSA-N N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C Chemical compound N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C IIGAAOXXRKTFAM-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 2
239000012972 dimethylethanolamine Substances 0.000 description 2
150000002433 hydrophilic molecules Chemical class 0.000 description 2
125000006850 spacer group Chemical group 0.000 description 2
238000013112 stability test Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
229960003080 taurine Drugs 0.000 description 2
ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 1
UEEJHVSXFDXPFK-UHFFFAOYSA-O N-dimethylethanolamine Chemical compound C[NH+](C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-O 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000007853 buffer solution Substances 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
229910000397 disodium phosphate Inorganic materials 0.000 description 1
235000019800 disodium phosphate Nutrition 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
HLJDOURGTRAFHE-UHFFFAOYSA-N isocyanic acid;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=O.N=C=O.CC1=CC(=O)CC(C)(C)C1 HLJDOURGTRAFHE-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000001488 sodium phosphate Substances 0.000 description 1
GWLWWNLFFNJPDP-UHFFFAOYSA-M sodium;2-aminoethanesulfonate Chemical group [Na+].NCCS([O-])(=O)=O GWLWWNLFFNJPDP-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
- C08G18/025—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing carbodiimide groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Dispersion Chemistry (AREA)
Polyurethanes Or Polyureas (AREA)
Paints Or Removers (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

RU2005141416/04A 2003-07-03 2004-07-02 Способ приготовления стабильных водных дисперсий поликарбодиимидов, которые не содержат органических растворителей и могут быть использованы в качестве поперечно-сшивающих агентов RU2313541C2 (ru)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL1023817A NL1023817C2 (nl)	2003-07-03	2003-07-03	Werkwijze voor de bereiding van stabiele polycarbodiimide dispersies in water, welke geen organische oplosmiddelen bevatten en als vernettingsmiddel kunnen worden gebruikt.
NL1023817		2003-07-03

Publications (2)

Publication Number	Publication Date
RU2005141416A RU2005141416A (ru)	2006-08-10
RU2313541C2 true RU2313541C2 (ru)	2007-12-27

Family

ID=33563077

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
RU2005141416/04A RU2313541C2 (ru)	2003-07-03	2004-07-02	Способ приготовления стабильных водных дисперсий поликарбодиимидов, которые не содержат органических растворителей и могут быть использованы в качестве поперечно-сшивающих агентов

Country Status (17)

Country	Link
US (1)	US7439316B2 (pl)
EP (1)	EP1644428B2 (pl)
JP (1)	JP5035792B2 (pl)
KR (1)	KR101132250B1 (pl)
CN (1)	CN100543056C (pl)
AU (1)	AU2004253814B2 (pl)
BR (1)	BRPI0411732B1 (pl)
CA (1)	CA2531230C (pl)
DK (1)	DK1644428T4 (pl)
ES (1)	ES2466382T5 (pl)
MX (1)	MXPA05013947A (pl)
NL (1)	NL1023817C2 (pl)
PL (1)	PL1644428T5 (pl)
PT (1)	PT1644428E (pl)
RU (1)	RU2313541C2 (pl)
WO (1)	WO2005003204A2 (pl)
ZA (1)	ZA200509360B (pl)

Cited By (2)

* Cited by examiner, † Cited by third party
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RU2543385C2 (ru) *	2009-05-15	2015-02-27	Райн Хеми Райнау ГмбХ	Способ получения карбодиимидов
RU2543385C9 (ru) *	2009-05-15	2016-02-20	Райн Хеми Райнау ГмбХ	Способ получения карбодиимидов

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US8389113B2 (en) *	2002-09-17	2013-03-05	Ppg Industries Ohio, Inc.	Substrates and articles of manufacture coated with a waterborne 2K coating composition
JP2006035190A (ja) *	2004-07-30	2006-02-09	Nisshinbo Ind Inc	硬化塗膜の製造方法
NL1031053C2 (nl) *	2006-02-02	2007-08-03	Stahl Int Bv	Werkwijze voor de bereiding van dispersies van vernettingsmiddelen in water.
CN101679705B (zh) *	2007-06-08	2013-12-11	3M创新有限公司	含氟烷基的酯低聚物与聚碳二亚胺的共混物
US20090246393A1 (en) *	2008-03-27	2009-10-01	Ppg Industries Ohio, Inc.	Polycarbodiimides
WO2010028217A1 (en) *	2008-09-05	2010-03-11	The Board Of Trustees Of The University Of Illinois	Poly(ethylene glycol) methyl ether carbodiimide coupling reagents for the biological and chemical functionalization of water soluble nanoparticles
US8900667B2 (en) *	2009-12-18	2014-12-02	Ppg Industries Ohio, Inc.	One-component, ambient curable waterborne coating compositions, related methods and coated substrates
MX2012010068A (es) *	2010-03-02	2012-12-17	Ppg Ind Ohio Inc	Composiciones de revestimiento de un componente, curables al ambiente, que cotienen agua, metodos relacionados y sustratos revestidos.
EP2371873A1 (de)	2010-04-01	2011-10-05	Bayer MaterialScience AG	Verfahren zur Carbodiimidisierung
NL2005163C2 (nl) *	2010-07-28	2012-01-31	Stahl Int Bv	Werkwijze voor de bereiding van multifunctionele polycarbodiimides, welke gebruikt worden als vernettingsmiddel.
EP2423186B1 (de) *	2010-08-30	2017-05-31	LANXESS Deutschland GmbH	Neuartige haftvermittler auf basis von carbodiimiden, haftvermittlerhaltige, wässrige resorcin-formaldehyd-latex-dispersionen, haftungsverbesserte fasern, verfahren zu deren herstellung und deren verwendung
JP5945172B2 (ja) *	2011-06-29	2016-07-05	三洋化成工業株式会社	樹脂改質剤
EP2660258A1 (de) *	2012-05-03	2013-11-06	Rhein Chemie Rheinau GmbH	Neue Carbodiimid-haltige Zusammensetzungen, ein Verfahren zu deren Herstellung und deren Verwendung
ES2571582T3 (es)	2012-05-24	2016-05-26	Basf Se	Composiciones acuosas de aglutinante
JP5922499B2 (ja) *	2012-05-31	2016-05-24	三洋化成工業株式会社	樹脂改質剤
WO2014044742A1 (en) *	2012-09-19	2014-03-27	Basf Se	Process for the purification of a polycarbodiimide
US20140242281A1 (en)	2013-02-28	2014-08-28	Ppg Industries Ohio, Inc.	Methods and compositions for coating substrates
US11008471B2 (en)	2015-03-03	2021-05-18	Solaris Technology Ltd	Waterborne light radiation absorbing polyurethane mixed polyester polymer coating system
CA2986417C (en)	2015-05-30	2022-11-08	Dpoint Technologies Inc.	Supported water vapor transport membrane comprising polyethylene oxide copolymer
MY180554A (en) *	2015-07-08	2020-12-02	Nisshinbo Chemical Inc	Carbodiimide-based aqueous resin crosslinking agent
CN107614557B (zh) *	2016-01-05	2018-10-12	三井化学株式会社	聚碳二亚胺组合物、聚碳二亚胺组合物的制造方法、水分散组合物、溶液组合物、树脂组合物及树脂固化物
MX2018008552A (es) *	2016-01-15	2018-08-23	Ppg Ind Ohio Inc	Una composicion de revestimiento que comprende un polvo disperso en un portador liquido.
US9957394B2 (en)	2016-09-07	2018-05-01	Ppg Industries Ohio, Inc.	Methods for preparing powder coating compositions
JP6984838B2 (ja) *	2016-12-27	2021-12-22	日清紡ケミカル株式会社	カルボキシル基含有水性樹脂組成物、成形体、及びポリカルボジイミド化合物の製造方法
EP3589713A4 (en)	2017-02-28	2020-12-30	3M Innovative Properties Company	POLYURETHANE ADHESIVE WITH CHEMICAL RESISTANCE
JP6485726B1 (ja) *	2017-09-25	2019-03-20	Dic株式会社	合成皮革の製造方法
EP3502157A1 (de) *	2017-12-21	2019-06-26	Covestro Deutschland AG	Wässrige polycarbodiimid-dispersion mit erhöhter lagerstabilität und verfahren zu ihrer herstellung
CN108003313B (zh) *	2017-12-21	2020-08-04	上海朗亿功能材料有限公司	一种嵌段型聚碳化二亚胺水性交联剂及其制备方法
JP7028401B2 (ja)	2018-02-23	2022-03-02	日清紡ケミカル株式会社	水性カルボジイミド含有液の製造方法
CN108715628B (zh) *	2018-06-22	2022-04-01	上海朗亿功能材料有限公司	一种脂环族聚碳化二亚胺抗水解剂及其制备方法
CN108863851A (zh) *	2018-07-13	2018-11-23	成都创世芯研科技有限公司	一种支化型水性碳化二亚胺型交联剂及其制备方法
JP7668615B2 (ja) *	2018-08-10	2025-04-25	三井化学株式会社	繊維処理用カルボジイミド架橋剤
WO2020031951A1 (ja) *	2018-08-10	2020-02-13	三井化学株式会社	ポリカルボジイミド組成物、ポリカルボジイミド組成物の製造方法、水分散組成物、溶液組成物、樹脂組成物、樹脂硬化物および繊維処理用カルボジイミド架橋剤
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MXPA05013947A (es)	2006-07-03
JP2007521360A (ja)	2007-08-02
JP5035792B2 (ja)	2012-09-26
NL1023817C2 (nl)	2005-01-04
PL1644428T5 (pl)	2024-07-15
CA2531230A1 (en)	2005-01-13
CA2531230C (en)	2011-01-18
PT1644428E (pt)	2014-06-24
CN100543056C (zh)	2009-09-23
US7439316B2 (en)	2008-10-21
CN1805984A (zh)	2006-07-19
EP1644428A2 (en)	2006-04-12
ES2466382T5 (es)	2024-10-04
RU2005141416A (ru)	2006-08-10
WO2005003204A2 (en)	2005-01-13
EP1644428B2 (en)	2024-05-08
ES2466382T3 (es)	2014-06-10
HK1094215A1 (zh)	2007-03-23
KR20060017609A (ko)	2006-02-24
DK1644428T4 (da)	2024-05-27
EP1644428B1 (en)	2014-04-16
DK1644428T3 (da)	2014-06-23
AU2004253814B2 (en)	2009-12-17
AU2004253814A1 (en)	2005-01-13
PL1644428T3 (pl)	2014-09-30
ZA200509360B (en)	2007-04-25
WO2005003204A3 (en)	2005-03-10
KR101132250B1 (ko)	2012-04-02
BRPI0411732B1 (pt)	2014-12-16
US20060106189A1 (en)	2006-05-18
BRPI0411732A (pt)	2006-08-08

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Date	Code	Title	Description
2013-04-27	MM4A	The patent is invalid due to non-payment of fees	Effective date: 20120703

Publication	Publication Date	Title
RU2313541C2 (ru)	2007-12-27	Способ приготовления стабильных водных дисперсий поликарбодиимидов, которые не содержат органических растворителей и могут быть использованы в качестве поперечно-сшивающих агентов
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EP0148970B1 (en)	1988-01-07	Stable, aqueous dispersions of polyurethane-ureas and coatings and films prepared therefrom
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US4335029A (en)	1982-06-15	Aqueous polyurethane compositions
CA1129129A (en)	1982-08-03	Process for the production of aqueous dispersions or solutions of polyurethane polyureas, and dispersions or solution obtainable by this process and their use
US4598121A (en)	1986-07-01	Cold-crosslinking polyurethane dispersions, manufacture and use of the same
EP0219677A1 (en)	1987-04-29	A process for the preparation of an aqueous polyurethane-urea dispersion
CA1102027A (en)	1981-05-26	Process for the preparation of aqueous dispersions or solutions of polyurethanes and the use thereof
EP1153052B1 (en)	2004-12-29	Process for the preparation of an aqueous dispersion of an anionic polyurethane free of volatile tertiary amines
TW201041922A (en)	2010-12-01	Functionalized polyurethanepolyurea dispersions
US5124400A (en)	1992-06-23	Aqueous polyurethane dispersions and adhesives based thereon
DE3227017A1 (de)	1984-01-26	Verfahren zur herstellung von kunststoffen aus polyisocyanat-basis
CA2079980C (en)	2003-02-11	Modified polyureas and a process for their production
CN100354329C (zh)	2007-12-12	聚氨酯树脂、水性聚氨酯树脂、亲水性改性剂、透湿性树脂及聚氨酯树脂的制造方法
DE3139966A1 (de)	1983-04-28	Verfahren zur herstellung von waessrigen dispersionen oder loesungen von polyurethanen, sowie deren verwendung zur herstellung von ueberzuegen und beschichtungen
JPH06220156A (ja)	1994-08-09	革の塗料のための、粘着性の低下したアニオン性修飾ポリウレタンウレア
EP3733728A1 (en)	2020-11-04	Aqueous polyurethane-urea dispersion
HK1094215B (en)	2010-05-28	Process for the preparation of stable polycarbodiimide dispersions in water, which are free of organic solvents and may be used as crosslinking agent
KR20210149041A (ko)	2021-12-08	수성 폴리우레탄-우레아 분산액
CN111748075A (zh)	2020-10-09	水性聚氨酯脲分散体

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